{ "meta": { "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.", "terms": "https://open.fda.gov/terms/", "license": "https://open.fda.gov/license/", "last_updated": "2026-07-30", "results": { "skip": 0, "limit": 10, "total": 6170 } }, "results": [ { "safetyreportversion": "2", "safetyreportid": "10019450", "primarysourcecountry": "US", "occurcountry": "US", "transmissiondateformat": "102", "transmissiondate": "20141212", "reporttype": "1", "serious": "2", "receivedateformat": "102", "receivedate": "20140318", "receiptdateformat": "102", "receiptdate": "20140410", "fulfillexpeditecriteria": "2", "companynumb": "US-TEVA-469314USA", "duplicate": "1", "reportduplicate": { "duplicatesource": "TEVA", "duplicatenumb": "US-TEVA-469314USA" }, "primarysource": { "reportercountry": "US", "qualification": "3" }, "sender": { "sendertype": "2", "senderorganization": "FDA-Public Use" }, "receiver": { "receivertype": "6", "receiverorganization": "FDA" }, "patient": { 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"064", "drugstartdateformat": "102", "drugstartdate": "20130410", "drugenddateformat": "102", "drugenddate": "20130607" } ] } }, { "safetyreportversion": "3", "safetyreportid": "10159408", "primarysourcecountry": "US", "occurcountry": "US", "transmissiondateformat": "102", "transmissiondate": "20151125", "reporttype": "1", "serious": "1", "seriousnesshospitalization": "1", "receivedateformat": "102", "receivedate": "20140508", "receiptdateformat": "102", "receiptdate": "20150804", "fulfillexpeditecriteria": "2", "companynumb": "US-BAYER-2014-065365", "duplicate": "1", "reportduplicate": { "duplicatesource": "BAYER", "duplicatenumb": "US-BAYER-2014-065365" }, "primarysource": { "reportercountry": "US", "qualification": "5" }, "sender": { "sendertype": "2", "senderorganization": "FDA-Public Use" }, "receiver": { "receivertype": "6", "receiverorganization": "FDA" }, "patient": { "patientonsetage": "28", "patientonsetageunit": "801", "patientagegroup": "5", "patientweight": "67.57", "patientsex": "2", "reaction": [ { "reactionmeddraversionpt": "18.1", "reactionmeddrapt": "Deep vein thrombosis", "reactionoutcome": "1" }, { "reactionmeddraversionpt": "18.1", "reactionmeddrapt": "Injury", "reactionoutcome": "1" }, { "reactionmeddraversionpt": "18.1", "reactionmeddrapt": "Pain", "reactionoutcome": "1" } ], "drug": [ { "drugcharacterization": "1", "medicinalproduct": "YAZ", "drugauthorizationnumb": "021676", "drugdosagetext": "UNK", "drugdosageform": "FILM-COATED TABLET", "drugindication": "CONTRACEPTION", "drugstartdateformat": "102", "drugstartdate": "20080710", "drugenddateformat": "102", "drugenddate": "20100513", "actiondrug": "1", "activesubstance": { "activesubstancename": "DROSPIRENONE\\ETHINYL ESTRADIOL" }, "openfda": { "application_number": [ "NDA021676" ], "brand_name": [ "YAZ" ], "generic_name": [ "DROSPIRENONE AND ETHINYL ESTRADIOL" ], "manufacturer_name": [ "Bayer HealthCare Pharmaceuticals Inc." ], "product_ndc": [ "50419-405" ], "product_type": [ "HUMAN PRESCRIPTION DRUG" ], "rxcui": [ "630734", "748797", "748798", "748856" ], "spl_id": [ "4f14f9c9-411b-48b0-a3d3-cac639cdfb8b" ], "spl_set_id": [ "065f33e4-b587-4e66-b896-ca9ab7b7c876" ], "package_ndc": [ "50419-405-03" ] } }, { "drugcharacterization": "2", "medicinalproduct": "SULFACETAMIDE SODIUM [SULFACETAMIDE]", "drugstructuredosagenumb": "10", "drugstructuredosageunit": "030", "drugdosagetext": "10 %, UNK", "drugadministrationroute": "061", "drugstartdateformat": "102", "drugstartdate": "20100409" }, { "drugcharacterization": "2", "medicinalproduct": "DIFFERIN", "drugstructuredosagenumb": ".3", "drugstructuredosageunit": "030", "drugdosagetext": "0.3 %, UNK", "drugadministrationroute": "061", "drugstartdateformat": "102", "drugstartdate": "20100409", "activesubstance": { "activesubstancename": "ADAPALENE" }, "openfda": { "application_number": [ "NDA020380", "NDA021753" ], "brand_name": [ "DIFFERIN" ], "generic_name": [ "ADAPALENE" ], "manufacturer_name": [ "Galderma Laboratories, 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"reactionmeddraversionpt": "17.1", "reactionmeddrapt": "Pneumonia", "reactionoutcome": "6" }, { "reactionmeddraversionpt": "17.1", "reactionmeddrapt": "Renal function test abnormal", "reactionoutcome": "6" }, { "reactionmeddraversionpt": "17.1", "reactionmeddrapt": "Off label use", "reactionoutcome": "6" }, { "reactionmeddraversionpt": "17.1", "reactionmeddrapt": "Dyspnoea", "reactionoutcome": "1" }, { "reactionmeddraversionpt": "17.1", "reactionmeddrapt": "Inappropriate schedule of drug administration", "reactionoutcome": "6" }, { "reactionmeddraversionpt": "17.1", "reactionmeddrapt": "Abscess", "reactionoutcome": "6" }, { "reactionmeddraversionpt": "17.1", "reactionmeddrapt": "Fluid overload", "reactionoutcome": "1" }, { "reactionmeddraversionpt": "17.1", "reactionmeddrapt": "Infection", "reactionoutcome": "2" }, { "reactionmeddraversionpt": "17.1", "reactionmeddrapt": "Tendon rupture", "reactionoutcome": "6" }, { "reactionmeddraversionpt": "17.1", "reactionmeddrapt": "Renal aneurysm", "reactionoutcome": "6" }, { "reactionmeddraversionpt": "17.1", "reactionmeddrapt": "Blood creatinine increased", "reactionoutcome": "2" }, { "reactionmeddraversionpt": "17.1", "reactionmeddrapt": "Vision blurred", "reactionoutcome": "2" }, { "reactionmeddraversionpt": "17.1", "reactionmeddrapt": "Oedematous kidney", "reactionoutcome": "6" }, { "reactionmeddraversionpt": "17.1", "reactionmeddrapt": "Hyperkalaemia", "reactionoutcome": "1" }, { "reactionmeddraversionpt": "17.1", "reactionmeddrapt": "Hydronephrosis", "reactionoutcome": "2" } ], "drug": [ { "drugcharacterization": "2", "medicinalproduct": "DEPAKINE /00228501/", "drugseparatedosagenumb": "1", "drugintervaldosageunitnumb": "1", "drugintervaldosagedefinition": "801", "drugdosagetext": "UNK, PRN", "drugadministrationroute": "048", "drugindication": "EPILEPSY", "drugstartdateformat": "102", "drugstartdate": "20101105", "activesubstance": { "activesubstancename": "VALPROIC ACID" } }, { "drugcharacterization": "2", "medicinalproduct": "LASIX", "drugseparatedosagenumb": "1", "drugintervaldosageunitnumb": "1", "drugintervaldosagedefinition": "801", "drugdosagetext": "UNK, PRN", "drugadministrationroute": "048", "drugindication": "DYSPNOEA", "drugstartdateformat": "102", "drugstartdate": "20111223", "drugenddateformat": "102", "drugenddate": "20120703", "activesubstance": { "activesubstancename": "FUROSEMIDE" }, "openfda": { "application_number": [ "NDA016273" ], "brand_name": [ "LASIX" ], "generic_name": [ "FUROSEMIDE" ], "manufacturer_name": [ "Validus Pharmaceuticals LLC" ], "product_ndc": [ "30698-060", "30698-067", "30698-066" ], "product_type": [ "HUMAN PRESCRIPTION DRUG" ], "route": [ "ORAL" ], "substance_name": [ "FUROSEMIDE" ], "rxcui": [ "197732", "200801", "200809", "205732", "310429", "313988" ], "spl_id": [ "4002943d-0b4b-4ff0-e063-6394a90ae63b" ], "spl_set_id": [ "2c9b4d8f-0770-482d-a9e6-9c616a440b1a" ], "package_ndc": [ "30698-067-01", "30698-067-10", "30698-060-01", "30698-060-10", 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"medicinalproduct": "ZITHROMAX", "drugseparatedosagenumb": "1", "drugintervaldosageunitnumb": "1", "drugintervaldosagedefinition": "801", "drugdosagetext": "UNK, PRN", "drugadministrationroute": "042", "drugindication": "PROPHYLAXIS", "drugstartdateformat": "102", "drugstartdate": "20120313", "drugenddateformat": "102", "drugenddate": "20120313", "activesubstance": { "activesubstancename": "AZITHROMYCIN DIHYDRATE" }, "openfda": { "application_number": [ "NDA050711", "NDA050784", "NDA050710", "NDA050733" ], "brand_name": [ "ZITHROMAX" ], "generic_name": [ "AZITHROMYCIN DIHYDRATE" ], "manufacturer_name": [ "Pfizer Laboratories Div Pfizer Inc" ], "product_ndc": [ "0069-3060", "0069-3070", "0069-3110", "0069-3120", "0069-3130", "0069-3140", "0069-4061", "0069-3150", "0069-0400" ], "product_type": [ "HUMAN PRESCRIPTION DRUG" ], "route": [ "ORAL", "INTRAVENOUS" ], "substance_name": [ "AZITHROMYCIN DIHYDRATE" ], "spl_id": [ "1c5f0fcc-88ce-47e9-a128-b7326b7a5a02", "73a19258-3cc4-49b1-8f18-e17fd418fe36", "87b9089f-c9cd-41c9-9358-29f6e4014af6" ], "spl_set_id": [ "db52b91e-79f7-4cc1-9564-f2eee8e31c45", "3b631aa1-2d46-40bc-a614-d698301ea4f9", "8d24bacb-feff-4c6a-b8df-625e1435387a" ], "package_ndc": [ "0069-3060-30", "0069-3060-75", "0069-3060-86", "0069-3070-30", "0069-3070-75", "0069-3110-19", "0069-3120-19", "0069-3130-19", "0069-3140-19", "0069-4061-01", "0069-4061-75", "0069-4061-89", "0069-3150-84", "0069-3150-83", "0069-0400-01", "0069-0400-10" ], "unii": [ "5FD1131I7S" ], "rxcui": [ "1668238", "1668240" ] } }, { "drugcharacterization": "2", "medicinalproduct": "ZITHROMAX", "drugseparatedosagenumb": "1", "drugintervaldosageunitnumb": "1", "drugintervaldosagedefinition": "801", "drugdosagetext": "UNK", "drugadministrationroute": "042", "drugstartdateformat": "102", "drugstartdate": "20120509", "drugenddateformat": "102", "drugenddate": "20120509", "activesubstance": { "activesubstancename": "AZITHROMYCIN DIHYDRATE" }, "openfda": { "application_number": [ "NDA050711", "NDA050784", "NDA050710", "NDA050733" ], "brand_name": [ "ZITHROMAX" ], "generic_name": [ "AZITHROMYCIN DIHYDRATE" ], "manufacturer_name": [ "Pfizer Laboratories Div Pfizer Inc" ], "product_ndc": [ "0069-3060", "0069-3070", "0069-3110", "0069-3120", "0069-3130", "0069-3140", "0069-4061", "0069-3150", "0069-0400" ], "product_type": [ "HUMAN PRESCRIPTION DRUG" ], "route": [ "ORAL", "INTRAVENOUS" ], "substance_name": [ "AZITHROMYCIN DIHYDRATE" ], "spl_id": [ "1c5f0fcc-88ce-47e9-a128-b7326b7a5a02", "73a19258-3cc4-49b1-8f18-e17fd418fe36", "87b9089f-c9cd-41c9-9358-29f6e4014af6" ], "spl_set_id": [ "db52b91e-79f7-4cc1-9564-f2eee8e31c45", "3b631aa1-2d46-40bc-a614-d698301ea4f9", "8d24bacb-feff-4c6a-b8df-625e1435387a" ], "package_ndc": [ "0069-3060-30", "0069-3060-75", "0069-3060-86", "0069-3070-30", "0069-3070-75", "0069-3110-19", "0069-3120-19", "0069-3130-19", "0069-3140-19", "0069-4061-01", "0069-4061-75", "0069-4061-89", "0069-3150-84", "0069-3150-83", "0069-0400-01", "0069-0400-10" ], "unii": [ "5FD1131I7S" ], "rxcui": [ "1668238", "1668240" ] } }, { "drugcharacterization": "2", "medicinalproduct": "VIBRAVENOS", "drugseparatedosagenumb": "1", "drugintervaldosageunitnumb": "1", "drugintervaldosagedefinition": "801", "drugdosagetext": "UNK, PRN", "drugadministrationroute": "048", "drugstartdateformat": "102", "drugstartdate": "20120616", "drugenddateformat": "102", "drugenddate": "20120625" }, { "drugcharacterization": "1", "medicinalproduct": "SOLIRIS", "drugauthorizationnumb": "125166", "drugstructuredosagenumb": "900", "drugstructuredosageunit": "003", "drugseparatedosagenumb": "1", "drugintervaldosageunitnumb": "1", "drugintervaldosagedefinition": "802", "drugdosagetext": "900 MG, QMONTH", "drugdosageform": "CONCENTRATE FOR SOLUTION FOR INFUSION", "drugadministrationroute": "042", "drugindication": "HAEMOLYTIC URAEMIC SYNDROME", "drugstartdateformat": "102", "drugstartdate": "20120313", "drugenddateformat": "102", "drugenddate": 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"brand_name": [ "DIFFERIN" ], "generic_name": [ "ADAPALENE" ], "manufacturer_name": [ "Galderma Laboratories, L.P." ], "product_ndc": [ "0299-4910", "0299-5918" ], "product_type": [ "HUMAN OTC DRUG", "HUMAN PRESCRIPTION DRUG" ], "route": [ "TOPICAL" ], "substance_name": [ "ADAPALENE" ], "rxcui": [ "153183", "307731", "722111", "722113" ], "spl_id": [ "7d2ef345-753e-4f6c-bb76-15fae398a44d", "cc125ed9-1ac8-491e-8eba-bd55426fc825" ], "spl_set_id": [ "0739d631-171b-42a8-bd55-0022b8df2d8a", "a0031324-92a6-4c11-90e2-c2818f7278ec" ], "package_ndc": [ "0299-4910-45", "0299-4910-15", "0299-4910-00", "0299-4910-10", "0299-4910-40", "0299-5918-45", "0299-5918-25", "0299-5918-15", "0299-5918-02" ], "nui": [ "N0000175607", "M0018962" ], "pharm_class_epc": [ "Retinoid [EPC]" ], "pharm_class_cs": [ "Retinoids [CS]" ], "unii": [ "1L4806J2QF" ] } }, { "drugcharacterization": "2", "medicinalproduct": "PROGRAF", "drugseparatedosagenumb": "1", "drugintervaldosageunitnumb": "1", "drugintervaldosagedefinition": "801", "drugdosagetext": "UNK, PRN", "drugadministrationroute": "048", "drugindication": "RENAL TRANSPLANT", "drugstartdateformat": "102", "drugstartdate": "20111223", "drugenddateformat": "102", "drugenddate": "20120703", "activesubstance": { "activesubstancename": "TACROLIMUS\\TACROLIMUS ANHYDROUS" }, "openfda": { "application_number": [ "NDA050708", "NDA210115", "NDA050709" ], "brand_name": [ "PROGRAF" ], "generic_name": [ "TACROLIMUS" ], "manufacturer_name": [ "Astellas Pharma US, Inc." ], "product_ndc": [ "0469-0607", "0469-0617", "0469-0657", "0469-3016", "0469-1230", "0469-1330" ], "product_type": [ "HUMAN PRESCRIPTION DRUG" ], "route": [ "ORAL", "INTRAVENOUS" ], "substance_name": [ "TACROLIMUS" ], "rxcui": [ "108513", "108514", "108515", "198377", "198378", "198379", "261134", "313190", "2052605", "2052609", "2052703", "2052704" ], "spl_id": [ "e9157663-1515-4ba3-83b5-1622cf6f0f99" ], "spl_set_id": [ "7f667de1-9dfa-4bd6-8ba0-15ee2d78873b" ], "package_ndc": [ "0469-0607-73", "0469-0617-73", "0469-0617-11", "0469-0657-73", "0469-0657-11", "0469-3016-01", "0469-1230-50", "0469-1330-50" ], "unii": [ "WM0HAQ4WNM" ] } } ], "summary": { "narrativeincludeclinical": "CASE EVENT DATE: 201112" } } }, { "safetyreportversion": "2", "safetyreportid": "10204887", "primarysourcecountry": "CA", "occurcountry": "CA", "transmissiondateformat": "102", "transmissiondate": "20141212", "reporttype": "1", "serious": "1", "seriousnesshospitalization": "1", "receivedateformat": "102", "receivedate": "20140529", "receiptdateformat": "102", "receiptdate": "20140529", "fulfillexpeditecriteria": "1", "companynumb": "CA-AMGEN-CANSP2014014978", "duplicate": "1", "reportduplicate": { "duplicatesource": "AMGEN", "duplicatenumb": "CA-AMGEN-CANSP2014014978" }, "primarysource": { "reportercountry": "CA", "qualification": "1" }, "sender": { "sendertype": "2", "senderorganization": "FDA-Public Use" }, "receiver": { "receivertype": "6", "receiverorganization": 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"reactionmeddrapt": "Decreased appetite", "reactionoutcome": "1" }, { "reactionmeddraversionpt": "17.0", "reactionmeddrapt": "Oropharyngeal pain", "reactionoutcome": "1" }, { "reactionmeddraversionpt": "17.0", "reactionmeddrapt": "Ear pain", "reactionoutcome": "1" }, { "reactionmeddraversionpt": "17.0", "reactionmeddrapt": "Rhinorrhoea", "reactionoutcome": "3" }, { "reactionmeddraversionpt": "17.0", "reactionmeddrapt": "Malaise", "reactionoutcome": "6" } ], "drug": [ { "drugcharacterization": "1", "medicinalproduct": "ENBREL", "drugauthorizationnumb": "103795", "drugstructuredosagenumb": "25", "drugstructuredosageunit": "003", "drugseparatedosagenumb": "2", "drugintervaldosageunitnumb": "1", "drugintervaldosagedefinition": "803", "drugdosagetext": "25 MG, 2 TIMES/WK", "drugdosageform": "POWDER AND SOLVENT FOR SOLUTION FOR INJECTION", "drugadministrationroute": "065", "drugindication": "JUVENILE IDIOPATHIC ARTHRITIS", "drugstartdateformat": "102", "drugstartdate": "20140110", 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"patientonsetageunit": "801", "patientsex": "1", "reaction": [ { "reactionmeddraversionpt": "17.1", "reactionmeddrapt": "Drug effect decreased", "reactionoutcome": "1" }, { "reactionmeddraversionpt": "17.1", "reactionmeddrapt": "Erythema", "reactionoutcome": "1" }, { "reactionmeddraversionpt": "17.1", "reactionmeddrapt": "Off label use", "reactionoutcome": "1" }, { "reactionmeddraversionpt": "17.1", "reactionmeddrapt": "Rash macular", "reactionoutcome": "1" } ], "drug": [ { "drugcharacterization": "1", "medicinalproduct": "MIRVASO", "drugbatchnumb": "105921", "drugauthorizationnumb": "204708", "drugstructuredosagenumb": "1", "drugstructuredosageunit": "032", "drugseparatedosagenumb": "1", "drugintervaldosageunitnumb": "1", "drugintervaldosagedefinition": "804", "drugdosagetext": "0.33%", "drugdosageform": "GEL", "drugadministrationroute": "061", "drugindication": "ROSACEA", "drugstartdateformat": "102", "drugstartdate": "20140401", "drugenddateformat": "102", "drugenddate": "20140403", "actiondrug": "1", "activesubstance": { "activesubstancename": "BRIMONIDINE TARTRATE" }, "openfda": { "application_number": [ "NDA204708" ], "brand_name": [ "MIRVASO" ], "generic_name": [ "BRIMONIDINE TARTRATE" ], "manufacturer_name": [ "Galderma Laboratories, L.P." ], "product_ndc": [ "0299-5980" ], "product_type": [ "HUMAN PRESCRIPTION DRUG" ], "route": [ "TOPICAL" ], "substance_name": [ "BRIMONIDINE TARTRATE" ], "rxcui": [ "1437707", "1437709" ], "spl_id": [ "253bf4a2-3c4d-f4af-e063-6394a90a0b0a" ], "spl_set_id": [ "f6a4353f-ae69-4214-901f-e5d42a6fbde7" ], "package_ndc": [ "0299-5980-30", "0299-5980-35", "0299-5980-45", "0299-5980-02", "0299-5980-00" ], "unii": [ "4S9CL2DY2H" ] } }, { "drugcharacterization": "1", "medicinalproduct": "MIRVASO", "drugbatchnumb": "105921", "drugauthorizationnumb": "204708", "drugstructuredosagenumb": "1", "drugstructuredosageunit": "032", "drugseparatedosagenumb": "1", "drugintervaldosageunitnumb": "1", "drugintervaldosagedefinition": "804", "drugdosagetext": "0.33%", "drugdosageform": "GEL", "drugadministrationroute": "061", "drugindication": "ERYTHEMA", "drugstartdateformat": "102", "drugstartdate": "20140401", "actiondrug": "1", "activesubstance": { "activesubstancename": "BRIMONIDINE TARTRATE" }, "openfda": { "application_number": [ "NDA204708" ], "brand_name": [ "MIRVASO" ], "generic_name": [ "BRIMONIDINE TARTRATE" ], "manufacturer_name": [ "Galderma Laboratories, L.P." ], "product_ndc": [ "0299-5980" ], "product_type": [ "HUMAN PRESCRIPTION DRUG" ], "route": [ "TOPICAL" ], "substance_name": [ "BRIMONIDINE TARTRATE" ], "rxcui": [ "1437707", "1437709" ], "spl_id": [ "253bf4a2-3c4d-f4af-e063-6394a90a0b0a" ], "spl_set_id": [ "f6a4353f-ae69-4214-901f-e5d42a6fbde7" ], "package_ndc": [ "0299-5980-30", "0299-5980-35", "0299-5980-45", "0299-5980-02", "0299-5980-00" ], "unii": [ "4S9CL2DY2H" ] } }, { "drugcharacterization": "2", "medicinalproduct": "CLINIQUE LOTION", "drugseparatedosagenumb": "1", "drugintervaldosageunitnumb": "1", "drugintervaldosagedefinition": "804", "drugadministrationroute": "061", "drugindication": "DRY SKIN PROPHYLAXIS", "drugstartdateformat": "602", "drugstartdate": "2009" }, { "drugcharacterization": "2", "medicinalproduct": "CLINIQUE SOAP", "drugseparatedosagenumb": "1", "drugintervaldosageunitnumb": "1", "drugintervaldosagedefinition": "804", "drugdosageform": "Cutaneous Stick", "drugadministrationroute": "061", "drugindication": "THERAPEUTIC SKIN CARE TOPICAL", "drugstartdateformat": "602", "drugstartdate": "2009" }, { "drugcharacterization": "2", "medicinalproduct": "DIFFERIN", "drugauthorizationnumb": "020748", "drugdosagetext": "0.1%", "drugdosageform": "CREAM", "drugindication": "ACNE", "activesubstance": { "activesubstancename": "ADAPALENE" }, "openfda": { "application_number": [ "NDA020380", "NDA021753" ], "brand_name": [ "DIFFERIN" ], "generic_name": [ "ADAPALENE" ], "manufacturer_name": [ "Galderma Laboratories, L.P." ], "product_ndc": [ "0299-4910", "0299-5918" ], "product_type": [ "HUMAN OTC DRUG", "HUMAN PRESCRIPTION DRUG" ], "route": [ "TOPICAL" ], "substance_name": [ "ADAPALENE" ], "rxcui": [ "153183", "307731", "722111", "722113" ], "spl_id": [ "7d2ef345-753e-4f6c-bb76-15fae398a44d", "cc125ed9-1ac8-491e-8eba-bd55426fc825" ], "spl_set_id": [ "0739d631-171b-42a8-bd55-0022b8df2d8a", "a0031324-92a6-4c11-90e2-c2818f7278ec" ], "package_ndc": [ "0299-4910-45", "0299-4910-15", "0299-4910-00", "0299-4910-10", "0299-4910-40", "0299-5918-45", "0299-5918-25", "0299-5918-15", "0299-5918-02" ], "nui": [ "N0000175607", "M0018962" ], "pharm_class_epc": [ "Retinoid [EPC]" ], "pharm_class_cs": [ "Retinoids [CS]" ], "unii": [ "1L4806J2QF" ] } } ], "summary": { "narrativeincludeclinical": "CASE EVENT DATE: 20140401" } } } ] }